Małgorzata Knapik, Anna Kusior, Magdalena Ziabka, Anita Trenczek-Zajac
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引用次数: 0
Abstract
The synthesis of BiVO4 multiphase photocatalysts was approached using a method and conditions designed to produce tetragonal-rich and monoclinic-rich materials with varying morphologies. The results of the SEM analysis indicated that a pH range of 3 to 7 during the hydrothermal process facilitates the formation of spherical particles with a diameter of 3.3–3.4 μm, comprising 6–7 nm crystals. Conversely, a pH value below 3 or the addition of CTAB as a surfactant resulted in the crystallization of nanocrystals with a size range of 0.5–5.0 μm, exhibiting well-defined facets. X-ray diffraction (XRD) analysis demonstrated that the former are predominantly tetragonal in variety, with a minor component of monoclinic. In the case of the latter, XRD in conjunction with electronic property analysis enabled the detection of the tetragonal variety in quantities below the detection threshold of the XRD, accompanied by the monoclinic variety. The monoclinic-rich BiVO4 exhibited notable discrepancies in its electrokinetic parameters, including hydrothermal diameter, in comparison to the tetragonal-rich samples. Moreover, PL studies revealed that the monoclinic-rich samples exhibited up to a 100-fold reduction in emissions, with a decay time up to six times longer which is attributed to the presence of point defects. Monoclinic-rich samples also demonstrate enhanced activity with regard to the degradation of Rhodamine B and basic Fuchsin. In particular, the former exhibits superior performance, achieving results that are several times more effective. Radical scavenging tests showed that •OH radicals were responsible for degrading bF and RhB dyes. The enhanced photocatalytic properties of monoclinic-rich samples were ascribed to augmented absorption, restricted recombination of charge carriers, and the existence of point defects.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.